Hydrogen Peroxide → 4-(Oxiran-2-yl)benzene-1-sulfonamide

HRID 23675

반응식

HRID 23675 반응식
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C(=O)([O-])[OH:14].[NH4+].OO>C(#N)C.O>[O:14]1[CH2:1][CH:2]1[C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:7][CH:8]=1

참가 물질

5

실험 절차

To a suspension of 4-sulfonamidostyrene (1.83 g, 0.01 mmol) and ammonium hydrogencarbonate (1.6 g, 0.02 mol) in acetonitrile/water (60 mL/30 mL) was added hydrogen peroxide (30% solution, 10 mL, 0.09). The mixture was kept in dark without stirring for 72 hours during which two portion of hydrogen peroxide (5 mL each) were introduced slowly. While HPLC showed all of the starting 4-sulfonamidostyrene was consumed, sodium thiosulfate solution (10%, 60 mL) was added slowly and stirred for 15 minutes. The mixture was extracted with dichloromethane (3×80 mL). The organic phases were combined, washed with brine and dried over magnesium sulfate. The solution was concentrated to give the crude title compound (0.52 g) as an oil.

후처리

  1. additionwere introduced slowly
  2. customwas consumed
  3. additionsodium thiosulfate solution (10%, 60 mL) was added slowly
  4. extractionThe mixture was extracted with dichloromethane (3×80 mL)
  5. washwashed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationThe solution was concentrated

출처 및 근거

ORD 기록
ord-54ff2e7e93da4edfaaa45a41cc0e4417
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06852731B2

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